PURPOSE OF THE REPORT: To evaluate the usefulness of F-18 fluoro-fluorodeoxygulose positron emission tomography computed tomography (F-18 FDG PET-CT) in detecting clinically defined active disease in patients with Takayasu arteritis. METHODS: F-18 FDG PET-CT was performed in 32 patients with Takayasu arteritis. Disease activity was assessed clinically by the National Institutes of Health (NIH) criteria. In 10 of the 32 patients, F-18 FDG PET-CT was performed while the patients were taking immunosuppressive drugs. Two nuclear physicians visually assessed the degree of F-18 FDG uptake in the walls of the aorta, its major branches and the pulmonary artery using a 4-point scale from grade 0 to III. F-18 FDG uptake greater than grade I in the thoracic aorta or greater than grade 0 in other areas were interpreted as active vasculitic lesions. RESULTS: Ten patients had active lesions on F-18 FDG PET-CT. According to the NIH criteria, 9 patients had active disease and 23 had inactive disease. Compared with disease activity assessed by the NIH criteria, F-18 FDG PET-CT had a sensitivity of 78% and a specificity of 87%. The erythrocyte sedimentation rate and CRP levels were significantly higher in F-18 FDG PET-CT-positive than in F-18 FDG PET-CT-negative patients. There was no significant difference in the proportion of positive PET scans according to the use of glucocorticoids. CONCLUSIONS: The sensitivity of F-18 FDG PET-CT for detecting active disease was higher in patients with higher erythrocyte sedimentation rate values. Although the specificity of F-18 FDG PET-CT was high, owing to the low sensitivity of the NIH criteria in detecting active disease, further studies are needed.
PURPOSE OF THE REPORT: To evaluate the usefulness of F-18 fluoro-fluorodeoxygulose positron emission tomography computed tomography (F-18 FDG PET-CT) in detecting clinically defined active disease in patients with Takayasu arteritis. METHODS:F-18 FDG PET-CT was performed in 32 patients with Takayasu arteritis. Disease activity was assessed clinically by the National Institutes of Health (NIH) criteria. In 10 of the 32 patients, F-18 FDG PET-CT was performed while the patients were taking immunosuppressive drugs. Two nuclear physicians visually assessed the degree of F-18 FDG uptake in the walls of the aorta, its major branches and the pulmonary artery using a 4-point scale from grade 0 to III. F-18 FDG uptake greater than grade I in the thoracic aorta or greater than grade 0 in other areas were interpreted as active vasculitic lesions. RESULTS: Ten patients had active lesions on F-18 FDG PET-CT. According to the NIH criteria, 9 patients had active disease and 23 had inactive disease. Compared with disease activity assessed by the NIH criteria, F-18 FDG PET-CT had a sensitivity of 78% and a specificity of 87%. The erythrocyte sedimentation rate and CRP levels were significantly higher in F-18 FDG PET-CT-positive than in F-18 FDG PET-CT-negative patients. There was no significant difference in the proportion of positive PET scans according to the use of glucocorticoids. CONCLUSIONS: The sensitivity of F-18 FDG PET-CT for detecting active disease was higher in patients with higher erythrocyte sedimentation rate values. Although the specificity of F-18 FDG PET-CT was high, owing to the low sensitivity of the NIH criteria in detecting active disease, further studies are needed.
Authors: Elena Incerti; Enrico Tombetti; Federico Fallanca; Elena M Baldissera; Pierpaolo Alongi; Elisabetta Tombolini; Silvia Sartorelli; Maria Grazia Sabbadini; Maurizio Papa; Francesco De Cobelli; Justin C Mason; Luigi Gianolli; Angelo A Manfredi; Maria Picchio Journal: Eur J Nucl Med Mol Imaging Date: 2017-02-08 Impact factor: 9.236
Authors: Haner Direskeneli; Sibel Z Aydin; Tanaz A Kermani; Eric L Matteson; Maarten Boers; Karen Herlyn; Raashid A Luqmani; Tuhina Neogi; Philip Seo; Ravi Suppiah; Gunnar Tomasson; Peter A Merkel Journal: J Rheumatol Date: 2011-07 Impact factor: 4.666
Authors: Peter C Grayson; Sara Alehashemi; Armin A Bagheri; Ali Cahid Civelek; Thomas R Cupps; Mariana J Kaplan; Ashkan A Malayeri; Peter A Merkel; Elaine Novakovich; David A Bluemke; Mark A Ahlman Journal: Arthritis Rheumatol Date: 2018-02-06 Impact factor: 10.995